Taiwan FDA registration 275f8a96690f31571dfabe2896924cec

Saibia Immunofixation Electrophoresis Daratumumab Test Kit

TW: 賽比亞 免疫固定電泳Daratumumab檢測套組
Taiwan flagTaiwan·Risk Class 2·SEBIA·Registered Jun 24, 2021 – Jun 24, 2026Expired
Registration details
Analysis ID
275f8a96690f31571dfabe2896924cec
Customs Code
DHA05603466708
Company information
Manufacturer
SEBIA
Manufacturer Country
France
Authorized Representative
ARQon Medtech Co., Ltd.
Product details
Intended Use
This product is paired with HYDRAGEL IF detection reagent and semi-automated HYDRASYS 2 electrophoresis equipment, HYDRAGEL IF detects monoclonal antibodies in human serum by immunofixation electrophoresis.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Jun 24, 2021
Expiry Date
Jun 24, 2026
Companies making similar products

Top companies providing products similar to "Saibia Immunofixation Electrophoresis Daratumumab Test Kit"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for Saibia Immunofixation Electrophoresis Daratumumab Test Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 275f8a96690f31571dfabe2896924cec and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SEBIA, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations